Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP1295050.RArPq8F4kFJLWSc3RoBpIvvG4PK3HokEHtRvy3Rb3z9Lc130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP1295050.RArPq8F4kFJLWSc3RoBpIvvG4PK3HokEHtRvy3Rb3z9Lc130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP1295050.RArPq8F4kFJLWSc3RoBpIvvG4PK3HokEHtRvy3Rb3z9Lc130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP1295050.RArPq8F4kFJLWSc3RoBpIvvG4PK3HokEHtRvy3Rb3z9Lc130_provenance.
- NP1295050.RArPq8F4kFJLWSc3RoBpIvvG4PK3HokEHtRvy3Rb3z9Lc130_assertion description "[For confirmation of homozygous protein C deficiency in a neonate with purpura fulminans or massive venous thrombosis, the infant should have undetectable protein C activity and both parents should be heterozygous for protein C deficiency.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1295050.RArPq8F4kFJLWSc3RoBpIvvG4PK3HokEHtRvy3Rb3z9Lc130_provenance.
- NP1295050.RArPq8F4kFJLWSc3RoBpIvvG4PK3HokEHtRvy3Rb3z9Lc130_assertion evidence source_evidence_literature NP1295050.RArPq8F4kFJLWSc3RoBpIvvG4PK3HokEHtRvy3Rb3z9Lc130_provenance.
- NP1295050.RArPq8F4kFJLWSc3RoBpIvvG4PK3HokEHtRvy3Rb3z9Lc130_assertion SIO_000772 2647943 NP1295050.RArPq8F4kFJLWSc3RoBpIvvG4PK3HokEHtRvy3Rb3z9Lc130_provenance.
- NP1295050.RArPq8F4kFJLWSc3RoBpIvvG4PK3HokEHtRvy3Rb3z9Lc130_assertion wasDerivedFrom befree-2016 NP1295050.RArPq8F4kFJLWSc3RoBpIvvG4PK3HokEHtRvy3Rb3z9Lc130_provenance.
- NP1295050.RArPq8F4kFJLWSc3RoBpIvvG4PK3HokEHtRvy3Rb3z9Lc130_assertion wasGeneratedBy ECO_0000203 NP1295050.RArPq8F4kFJLWSc3RoBpIvvG4PK3HokEHtRvy3Rb3z9Lc130_provenance.
- befree-2016 importedOn "2016-02-19" NP1295050.RArPq8F4kFJLWSc3RoBpIvvG4PK3HokEHtRvy3Rb3z9Lc130_provenance.